A Caveat in the Application of the Exciton Chirality Method to N,N-Dialkyl Amides. Synthesis and Structural Revision of AT2433-B1-Reference-Cited by-同舟云学术

A Caveat in the Application of the Exciton Chirality Method to N,N-Dialkyl Amides. Synthesis and Structural Revision of AT2433-B1

Published:1999-04-01 Issue:15 Volume:121 Page:3801-3802
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Chisholm John D.¹,Golik Jerzy¹,Krishnan Bala¹,Matson James A.¹,Van Vranken David L.¹

Affiliation:

1. Department of Chemistry, University of California Irvine, California 92697 Bristol-Myers Squibb Pharmaceutical Research Institute 5 Research Parkway, Wallingford, Connecticut 06492-7660

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9842924

Reference21 articles.

1. Nakanishi, K.; Berova, N. InCircular Dichroism: Principles and Applications; Nakanishi, K., Berova, N., Woody, R. W., Eds.; VCH: New York, 1994; p 361.

2. Circular dichroism due to exciton coupling between two 1-aryltriazene chromophores

3. AT2433-A1, AT2433A2, AT2433-B1 and AT2433-B2 novel antitumor compounds produced by Actinomadura melliaura. II. Structure determination.

4. AT2433-A1, AT2433-A2, AT2433-B1, and AT2433-B2 novel antitumor antibiotic compounds produced by Actinomadura melliaura. Taxonomy, fermentation, isolation and biological properties.

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